Associated Papers
Chitotriosidase gene polymorphisms and mutations limit the determination of chitotriosidase expression in sarcoidosis.
Csongrádi A et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2021
Chitotriosidase on treatment-naïve patients with Gaucher disease: A genotype vs phenotype study.
Sperb-Ludwig F et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2019
The Genetic Polymorphisms of 24 Base Pair Duplication and Point G102S of Human Chitotriosidase to Bancroftian Filariasis at the Thai⁻Myanmar Border.
Sanprasert V et al.
Pathogens (basel, Switzerland), 2019
Chitotriosidase deficiency in the Cypriot population: Identification of a novel deletion in the CHIT1 gene.
Mavrikiou G et al.
Clinical Biochemistry, 2016
Dup-24 bp in the CHIT1 Gene in Six Mexican Amerindian Populations.
Da Silva-José TD et al.
Jimd Reports, 2015
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites.
Manno N et al.
Carbohydrate Polymers, 2014
HGV&TB: a comprehensive online resource on human genes and genetic variants associated with tuberculosis.
Sahajpal R et al.
Database : the Journal of Biological Databases and Curation, 2014
25502817 (PubMed )
Supplement: bau112_Supplementary_Data.zip › Supplementary_Table_1.doc
Biochemical and Molecular Chitotriosidase Profiles in Patients with Gaucher Disease Type 1 in Minas Gerais, Brazil: New Mutation in CHIT1 Gene.
Adelino TER et al.
Jimd Reports, 2013
Chitotriosidase deficiency: a mutation update in an african population.
Arndt S et al.
Jimd Reports, 2013
Chitotriosidase deficiency in Brazil: evaluation of enzyme activity and genotypes.
Rodrigues MD et al.
Blood Cells, Molecules & Diseases, 2010
The chitinase and chitinase-like proteins: a review of genetic and functional studies in asthma and immune-mediated diseases.
Ober C et al.
Current Opinion in Allergy and Clinical Immunology, 2009
Type 1 Gaucher disease: null and hypomorphic novel chitotriosidase mutations-implications for diagnosis and therapeutic monitoring.
Grace ME et al.
Human Mutation, 2007
Human chitotriosidase polymorphisms G354R and A442V associated with reduced enzyme activity.
Lee P et al.
Blood Cells, Molecules & Diseases, 0
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